Device recall
Z-1599-2023: UA WIN 10 Kit, Catalog Number C52900, in-vitro diagnostic device, urine analysis
FDA device recall · Class II · Beckman Coulter, Inc.
Key facts
| Recall number (Z-number) | Z-1599-2023 |
|---|---|
| Recall event | 92056 |
| Product | UA WIN 10 Kit, Catalog Number C52900, in-vitro diagnostic device, urine analysis |
| Product code | KQO |
| Recalling firm | Beckman Coulter, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K022774 |
| FEI number | 3000203293 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database